A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676674



Internal ID21198523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40982192..40982242hg38UCSC Ensembl
chr4:40984209..40984259hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809547
Supporting Variants
Samples
Known GenesAPBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676674
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.4375


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